| Literature DB >> 27431056 |
Venn Vutey1, Silvia Castelli1, Ilda D'Annessa1, Luciana B P Sâmia2, Elaine M Souza-Fagundes2, Heloisa Beraldo2, Alessandro Desideri3.
Abstract
The human topoisomerase IB inhibition and the antiproliferative activity of 3-(4-bromophenyl)-1-pyridin-2-ylprop-2-en-1-one thiosemicarbazone HPyCT4BrPh alone and its copper(II) complex [Cu(PyCT4BrPh)Cl] was investigated. [Cu(PyCT4BrPh)Cl] inhibits both the DNA cleavage and religation step of the enzyme, whilst the ligand alone does not display any effect. In addition we show that coordination to copper(II) improves the cytotoxicity of HPyCT4BrPh against THP-1 leukemia and MCF-7 breast cancer cells. The data indicate that the copper(II) thiosemicarbazone complex may hit human topoisomerase IB and that metal coordination can be useful to improve cytotoxicity of this versatile class of compounds.Entities:
Keywords: Catalytic inhibitor; Copper(II) complex; Cytotoxicity; Human DNA topoisomerase IB; Molecular docking; Thiosemicarbazone
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Year: 2016 PMID: 27431056 DOI: 10.1016/j.abb.2016.07.009
Source DB: PubMed Journal: Arch Biochem Biophys ISSN: 0003-9861 Impact factor: 4.013